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rdf:type
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Description
| - Mutations of BCR-ABL tyrosine kinase domain represent the most frequently identified and best-studied mechanism of chronic myeloid leukemia (CML) resistance to the treatment with tyrosine kinase inhibitors (TKIs). In previously reported patients with F317L BCR-ABL kinasedomain mutation response to dasatinib treatment was invariably poor. We describe a CML patient in chronic phase with F317L mutation identified shortly after the initiation of dasatinib therapy,following previous imatinib failure. Despite a continual persistence of the F317L mutation, thepatient achieved a complete cytogenetic and a major molecular response after 4 and 6 months of dasatinib treatment, respectively, and maintained the response for more than 20 months of followup.Possible explanations for this long-term favourable response may include immune-mediatedeffects associated with dasatinib therapy, elimination of proliferative advantage of F317L-mutant cells through inhibition of Src family of kinases (SFK) or the presence of F3
- Mutations of BCR-ABL tyrosine kinase domain represent the most frequently identified and best-studied mechanism of chronic myeloid leukemia (CML) resistance to the treatment with tyrosine kinase inhibitors (TKIs). In previously reported patients with F317L BCR-ABL kinasedomain mutation response to dasatinib treatment was invariably poor. We describe a CML patient in chronic phase with F317L mutation identified shortly after the initiation of dasatinib therapy,following previous imatinib failure. Despite a continual persistence of the F317L mutation, thepatient achieved a complete cytogenetic and a major molecular response after 4 and 6 months of dasatinib treatment, respectively, and maintained the response for more than 20 months of followup.Possible explanations for this long-term favourable response may include immune-mediatedeffects associated with dasatinib therapy, elimination of proliferative advantage of F317L-mutant cells through inhibition of Src family of kinases (SFK) or the presence of F3 (en)
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Title
| - Major molecular response achieved with dasatinib in a CML patient with F317L BCR-ABL kinase domain mutation
- Major molecular response achieved with dasatinib in a CML patient with F317L BCR-ABL kinase domain mutation (en)
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skos:prefLabel
| - Major molecular response achieved with dasatinib in a CML patient with F317L BCR-ABL kinase domain mutation
- Major molecular response achieved with dasatinib in a CML patient with F317L BCR-ABL kinase domain mutation (en)
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skos:notation
| - RIV/61989592:15110/09:00009742!RIV10-MSM-15110___
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http://linked.open...avai/riv/aktivita
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http://linked.open...avai/riv/aktivity
| - P(NS9949), Z(MSM6198959205), Z(MSM6198959223)
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http://linked.open...iv/cisloPeriodika
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http://linked.open...vai/riv/dodaniDat
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http://linked.open...aciTvurceVysledku
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http://linked.open.../riv/druhVysledku
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http://linked.open...iv/duvernostUdaju
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http://linked.open...titaPredkladatele
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http://linked.open...dnocenehoVysledku
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http://linked.open...ai/riv/idVysledku
| - RIV/61989592:15110/09:00009742
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http://linked.open...riv/jazykVysledku
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http://linked.open.../riv/klicovaSlova
| - chronic myeloid leukemia; F317L BCR-ABL mutation; dasatinib; tyrosine kinase inhibitors (en)
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http://linked.open.../riv/klicoveSlovo
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http://linked.open...odStatuVydavatele
| - GB - Spojené království Velké Británie a Severního Irska
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http://linked.open...ontrolniKodProRIV
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http://linked.open...i/riv/nazevZdroje
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http://linked.open...in/vavai/riv/obor
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http://linked.open...ichTvurcuVysledku
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http://linked.open...cetTvurcuVysledku
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http://linked.open...vavai/riv/projekt
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http://linked.open...UplatneniVysledku
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http://linked.open...v/svazekPeriodika
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http://linked.open...iv/tvurceVysledku
| - Faber, Edgar
- Indrák, Karel
- Jarošová, Marie
- Divoká, Martina
- Rožmanová, Šárka
- Mojzíková, Renáta
- Plachý, Radek
- Šťastný, Marek
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http://linked.open...n/vavai/riv/zamer
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issn
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number of pages
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http://localhost/t...ganizacniJednotka
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